NCCAM Clinical Research Toolbox
The purpose of the NCCAM Clinical Research Toolbox is to provide a Web-based information repository for investigators and staff involved in NCCAM-funded clinical research. The Toolbox contains templates, sample forms, and information materials to assist clinical investigators in the development and conduct of high-quality clinical research studies.
Required Elements Prior to Starting Clinical Studies
The following documents must be submitted to NCCAM for approval prior to starting any NCCAM-funded clinical study:
- Protocol Document
- Case Report Forms
- Informed Consent
- Data and Safety Monitoring (DSM) Plan
- Natural Product Information (if applicable)
- Device Information (if applicable)
Other Elements for Clinical Studies
On-Site Monitoring FAQs and Checklists
- NCCAM Site Monitoring Visits
- Site Initiation Checklist (106KB PDF)
- Interim Site Visit Checklist (105KB PDF)
- Closeout Site Visit Checklist (115KB PDF)
Additional Tools and Resources
* Note: PDF files require a viewer such as the free Adobe Reader.